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    • 5. 发明申请
    • Method for implanting prosthetic valves
    • 植入人工瓣膜的方法
    • US20060259128A1
    • 2006-11-16
    • US11404439
    • 2006-04-14
    • Dusan PavcnikBrian CaseRam PaulJacob Flagle
    • Dusan PavcnikBrian CaseRam PaulJacob Flagle
    • A61F2/06
    • A61F2/2412A61F2/2427A61F2/2475A61F2250/0002A61F2250/0096
    • Methods for implanting a prosthetic valve in a body vessel having a fluid flow therethrough are provided. One method includes identifying a position of an existing valve and determining a factor affecting fluid flow in at least one of a first direction and a second direction at the existing valve. The method includes selecting the implantation position for a prosthetic valve at a distance away from the existing valve position in consideration of the factor. The method further includes providing the prosthetic valve for delivery to the implantation position, delivering and implanting the prosthetic valve at the position. The prosthetic valve includes at least one flexible member movable between a first position that permits fluid flow in the first direction and the second position that substantially prevents fluid flow in a second direction.
    • 提供了将人造瓣植入具有流体流体的体内容器中的方法。 一种方法包括识别现有阀的位置并且确定影响现有阀处的第一方向和第二方向中的至少一个中的流体流动的因素。 该方法包括考虑到该因素,在离开现有阀位置的距离处选择假体瓣膜的植入位置。 该方法还包括提供用于输送到植入位置的人造瓣膜,将该假体瓣膜输送和植入该位置。 假体瓣膜包括至少一个柔性构件,其可在第一位置和第二位置之间移动,所述第一位置允许流体在第一方向上流动,而第二位置基本上防止流体沿第二方向流动。
    • 8. 发明申请
    • Percutaneously placed prosthesis with thromboresistant valve portion
    • 经皮放置假体与抗血栓阀部分
    • US20050182483A1
    • 2005-08-18
    • US11056903
    • 2005-02-11
    • Thomas OsborneBrian CaseJacob FlagleGrant Hoffman
    • Thomas OsborneBrian CaseJacob FlagleGrant Hoffman
    • A61F2/06A61F2/24
    • A61F2/2424A61F2/2403A61F2/2418A61F2/2475A61F2220/0016A61F2220/005A61F2220/0058A61F2230/0054A61F2230/0078A61F2230/008
    • A venous valve prosthesis having a substantially non-expandable, valve portion comprising a valve-closing mechanism, such as a pair of opposing leaflets; and an anchoring portion, such as one or more self-expanding frames or stents that are expandable to anchor the prosthesis at the implantation site. In one embodiment, the rigid valve portion includes a deposition of material such as pyrolitic carbon to reduce the thrombogenecity of the blood-contacting surfaces. The anchoring portions preferably include a covering, such as a tubular construct of synthetic or collagen-derived material (such as a bioremodelable ECM material), which attaches about the support structure such that blood flow is directed through the valve mechanism as it transitions from the larger diameter anchoring portion to the intermediate, smaller-diameter portion of the prosthesis. In another embodiment, the valve support housing and valve-closing elements are delivered in a collapsed, folded, and/or dissembled state sized for delivery, then manipulated in situ to the second expanded configured following deployment.
    • 一种静脉瓣膜假体,其具有基本上不可扩张的阀部分,其包括阀关闭机构,例如一对相对的传单; 以及锚固部分,例如一个或多个自扩张框架或支架,其可扩张以在植入部位处锚固假体。 在一个实施例中,刚性瓣膜部分包括诸如热解碳的材料的沉积,以降低血液接触表面的血栓形成。 锚定部分优选地包括覆盖物,例如由合成或胶原衍生的材料(例如生物可重构的ECM材料)组成的管状构件,其附接在支撑结构上,使得当血液流过 较大直径的锚固部分到假体的中间较小直径部分。 在另一个实施例中,阀支撑壳体和阀关闭元件以折叠,折叠和/或拆卸状态被输送,其尺寸适于输送,然后在原位操作到第二扩张配置的后续部署。